Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  51 results for ""Aromatase deficiency""

Your Filters

Subject : genetic mutation
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation.

Subjects: ADRENOCORTICOTROPIC hormone; ADRENOGENITAL syndrome; GENETIC mutation

  • Source: Journal of Clinical Research in Pediatric Endocrinology; Jun2019, Vol. 11 Issue 2, p196-201, 6p

Record details

Read More Add to Saved list
×
Academic Journal

Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene.

Subjects: DEFICIENCY diseases; GENETIC polymorphisms; KARYOTYPES

  • Source: Journal of Clinical Research in Pediatric Endocrinology; Mar2020, Vol. 12 Issue 1, p109-112, 4p

Record details

Read More Add to Saved list
×
Academic Journal

Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene.

Subjects: DIAGNOSIS of deficiency diseases; DEFICIENCY diseases; OVARY abnormalities

  • Source: Journal of Clinical Research in Pediatric Endocrinology; Dec2018, Vol. 10 Issue 4, p377-381, 5p

Record details

Read More Add to Saved list
×
Academic Journal

Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous Genitalia.

Subjects: ADRENOGENITAL syndrome; AROMATASE; RARE diseases

  • Source: Sexual Development; Nov2017, Vol. 11 Issue 5/6, p275-279, 5p

Record details

Read More Add to Saved list
×
Academic Journal

A case of Aromatase deficiency due to a novel CYP19A1 mutation.

Subjects: TURNER'S syndrome; ANDROGENS; DIFFERENTIAL diagnosisINDIA

  • Source: BMC Endocrine Disorders; 2014, Vol. 14 Issue 1, p1-16, 16p, 1 Black and White Photograph, 1 Chart, 1 Graph

Record details

Read More Add to Saved list
×
Academic Journal

Aromatase Deficiency, a Rare Syndrome: Case Report.

Subjects: AROMATASE; GENETIC mutation; ESTROGEN

  • Source: Journal of Clinical Research in Pediatric Endocrinology; Jun2013, Vol. 5 Issue 2, p129-132, 4p, 1 Black and White Photograph, 1 Diagram, 1 Chart, 1 Graph

Record details

Read More Add to Saved list
×
Academic Journal

The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues.

Subjects: CYTOCHROME P-450; AROMATASE; PHENOTYPES

  • Source: Clinical Endocrinology; Nov2007, Vol. 67 Issue 5, p698-705, 8p, 3 Black and White Photographs, 2 Diagrams

Record details

Read More Add to Saved list
×
Academic Journal

Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans.

Subjects: VULVAR diseases; OVARY abnormalities; FETAL abnormalitiesTURKEY

  • Source: Journal of Clinical Research in Pediatric Endocrinology; Jun2016, Vol. 8 Issue 2, p205-210, 6p

Record details

Read More Add to Saved list
×
Academic Journal

Ovarian and uterine development and hormonal feedback mechanism in a 46 XX patient with CYP19A1 deficiency under low dose estrogen replacement.

Subjects: AROMATASE; ESTROGEN; ANDROGENS

  • Source: Gynecological Endocrinology; May2015, Vol. 31 Issue 5, p349-354, 6p

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization.

Subjects: *AROMATASE; *GENETIC mutation; *PHENOTYPES

  • Source: Molecular & Cellular Endocrinology. Sep2016, Vol. 433, p66-74. 9p.

Record details

Read More Add to Saved list
×
  • 1-10 of  51 results for ""Aromatase deficiency""